Hasil Pencarian - Veerle Labarque

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  1. 1
    Systematic Review of Genetic Modifiers Associated with the Development and/or Progression of Nephropathy in Patients with Sickle Cell Disease

    Systematic Review of Genetic Modifiers Associated with the Development and/or Progression of Nephropathy in Patients with Sickle Cell Disease oleh Veerle Labarque, Emmanuel Chide Okocha

    Diterbitkan 2024-05-01
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  2. 2
    Hemostatic phenotypes and genetic disorders

    Hemostatic phenotypes and genetic disorders oleh Fabienne Ver Donck, Veerle Labarque, Kathleen Freson

    Diterbitkan 2021-12-01
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  3. 3
    Physician decision-making process about withholding/withdrawing life-sustaining treatments in paediatric patients: a systematic review of qualitative evidence

    Physician decision-making process about withholding/withdrawing life-sustaining treatments in paediatric patients: a systematic review of qualitative evidence oleh Yajing Zhong, Alice Cavolo, Veerle Labarque, Chris Gastmans

    Diterbitkan 2022-06-01
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  4. 4
    Physicians’ attitudes and experiences about withholding/withdrawing life-sustaining treatments in pediatrics: a systematic review of quantitative evidence

    Physicians’ attitudes and experiences about withholding/withdrawing life-sustaining treatments in pediatrics: a systematic review of quantitative evidence oleh Yajing Zhong, Alice Cavolo, Veerle Labarque, Chris Gastmans

    Diterbitkan 2023-09-01
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  5. 5
    Subconjunctival Hemorrhage in a Child with the Blue Rubber Bleb Nevus Syndrome on Treatment with Oral Propranolol

    Subconjunctival Hemorrhage in a Child with the Blue Rubber Bleb Nevus Syndrome on Treatment with Oral Propranolol oleh Karen De Loecker, Veerle Labarque, Hilde Seynaeve, Ingele Casteels

    Diterbitkan 2021-05-01
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  6. 6
    Chinese and Belgian pediatricians’ perspectives toward pediatric palliative care: an online survey

    Chinese and Belgian pediatricians’ perspectives toward pediatric palliative care: an online survey oleh Yajing Zhong, Alice Cavolo, Veerle Labarque, Bernadette Dierckx de Casterlé, Chris Gastmans

    Diterbitkan 2024-04-01
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  7. 7
    Long-Term Outcome of Single-Session, Ultrasound-Guided, Radiofrequency Ablation for Symptomatic Small, Lower Limb, Venous Malformations

    Long-Term Outcome of Single-Session, Ultrasound-Guided, Radiofrequency Ablation for Symptomatic Small, Lower Limb, Venous Malformations oleh Laurence Verhaeghe, Veerle Labarque, Jan Vranckx, Inge Fourneau, Steven Pans, Geert Maleux

    Diterbitkan 2022-07-01
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  8. 8
    Case report: Cardiac intimal sarcoma in a young child

    Case report: Cardiac intimal sarcoma in a young child oleh Sanne Verbeek, Raf Sciot, Maria Debiec-Rychter, Veerle Labarque, Bart Meyns, Bjorn Cools

    Diterbitkan 2023-09-01
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  9. 9
    Factor VIII genotype and the risk of developing high-responding or low-responding inhibitors in severe hemophilia A: data from the PedNet Hemophilia Cohort of 1,202 children

    Factor VIII genotype and the risk of developing high-responding or low-responding inhibitors in severe hemophilia A: data from the PedNet Hemophilia Cohort of 1,202 children oleh Nadine G. Andersson, Veerle Labarque, Mutlu Kartal-Kaess, Fernando Pinto, Torben Stamm Mikkelsen, Rolf Ljung, PedNet Study Group

    Diterbitkan 2023-10-01
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  10. 10
    Methylene tetrahydrofolate reductase A1298C polymorphisms influence the adult sequelae of chemotherapy in childhood-leukemia survivors.

    Methylene tetrahydrofolate reductase A1298C polymorphisms influence the adult sequelae of chemotherapy in childhood-leukemia survivors. oleh Iris Elens, Sabine Deprez, Thibo Billiet, Charlotte Sleurs, Veerle Labarque, Anne Uyttebroeck, Stefaan Van Gool, Jurgen Lemiere, Rudi D'Hooge

    Diterbitkan 2021-01-01
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  11. 11
    Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction.

    Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction. oleh Benedetta Izzi, Inge Francois, Veerle Labarque, Chantal Thys, Christine Wittevrongel, Koen Devriendt, Eric Legius, Annick Van den Bruel, Marc D'Hooghe, Diether Lambrechts, Francis de Zegher, Chris Van Geet, Kathleen Freson

    Diterbitkan 2012-01-01
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  12. 12
    Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia

    Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia oleh Tadbir K. Bariana, Veerle Labarque, Jessica Heremans, Chantal Thys, Mara De Reys, Daniel Greene, Benjamin Jenkins, Luigi Grassi, Denis Seyres, Frances Burden, Deborah Whitehorn, Olga Shamardina, Sofia Papadia, Keith Gomez, NIHR BioResource, Chris Van Geet, Albert Koulman, Willem H. Ouwehand, Cedric Ghevaert, Mattia Frontini, Ernest Turro, Kathleen Freson

    Diterbitkan 2019-05-01
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  13. 13
    LIN28B is over-expressed in specific subtypes of pediatric leukemia and regulates lncRNA H19

    LIN28B is over-expressed in specific subtypes of pediatric leukemia and regulates lncRNA H19 oleh Hetty H. Helsmoortel, Barbara De Moerloose, Tim Pieters, Farzaneh Ghazavi, Silvia Bresolin, Hélène Cavé, Andrica de Vries, Valerie de Haas, Christian Flotho, Veerle Labarque, Charlotte Niemeyer, Pascale De Paepe, Nadine Van Roy, Jan Stary, Marry M. van den Heuvel-Eibrink, Yves Benoit, Johannes Schulte, Steven Goossens, Geert Berx, Jody J. Haigh, Frank Speleman, Pieter Van Vlierberghe, Tim Lammens

    Diterbitkan 2016-06-01
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